Bruce Castle

2.4k total citations
16 papers, 386 citations indexed

About

Bruce Castle is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Bruce Castle has authored 16 papers receiving a total of 386 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Bruce Castle's work include Genomic variations and chromosomal abnormalities (3 papers), Genetic Syndromes and Imprinting (2 papers) and Immunodeficiency and Autoimmune Disorders (2 papers). Bruce Castle is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetic Syndromes and Imprinting (2 papers) and Immunodeficiency and Autoimmune Disorders (2 papers). Bruce Castle collaborates with scholars based in United Kingdom, Australia and New Zealand. Bruce Castle's co-authors include P. J. BOWELL, I.Z. MacKenzie, Shaun P. Brennecke, Jane F. Ferguson, Peter D. Turnpenny, A. C. Turnbull, Laurence M. Demers, M. Selinger, I.Z. MacKenzie and Richard Caswell and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Obstetrics and Gynecology and BJOG An International Journal of Obstetrics & Gynaecology.

In The Last Decade

Bruce Castle

16 papers receiving 378 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Bruce Castle United Kingdom	13	197	186	113	48	33	16	386
Rikke Søe Denmark	5	32 0.2×	142 0.8×	82 0.7×	22 0.5×	78 2.4×	6	357
Sabine Hentze Germany	11	139 0.7×	178 1.0×	60 0.5×	64 1.3×	8 0.2×	18	412
Kazuso Iinuma Japan	13	183 0.9×	144 0.8×	148 1.3×	31 0.6×	8 0.2×	33	467
María Juliana Ballesta‐Martínez Spain	14	274 1.4×	308 1.7×	82 0.7×	20 0.4×	6 0.2×	33	569
Linus A. Völker Germany	10	46 0.2×	126 0.7×	22 0.2×	30 0.6×	10 0.3×	26	274
George Rebello South Africa	10	67 0.3×	158 0.8×	106 0.9×	7 0.1×	8 0.2×	25	316
Alida C. Knegt Netherlands	14	257 1.3×	271 1.5×	232 2.1×	13 0.3×	35 1.1×	35	652
Steven Schonberg United States	13	147 0.7×	247 1.3×	111 1.0×	21 0.4×	6 0.2×	19	422
Marija Volk Slovenia	14	115 0.6×	155 0.8×	76 0.7×	27 0.6×	63 1.9×	36	378
Tracy N. Hadnott United States	7	507 2.6×	333 1.8×	107 0.9×	9 0.2×	7 0.2×	11	752

Countries citing papers authored by Bruce Castle

Since Specialization

Citations

This map shows the geographic impact of Bruce Castle's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Bruce Castle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bruce Castle more than expected).

Fields of papers citing papers by Bruce Castle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bruce Castle. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Bruce Castle. The network helps show where Bruce Castle may publish in the future.

Co-authorship network of co-authors of Bruce Castle

This figure shows the co-authorship network connecting the top 25 collaborators of Bruce Castle. A scholar is included among the top collaborators of Bruce Castle based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Bruce Castle. Bruce Castle is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Smith, Philip, Hannah D. West, James Whitworth, et al.. (2020). Pathogenic germline variants in patients with features of hereditary renal cell carcinoma: Evidence for further locus heterogeneity. Genes Chromosomes and Cancer. 60(1). 5–16. 12 indexed citations

Burren, Christine, Richard Caswell, Bruce Castle, et al.. (2018). TRPV6 compound heterozygous variants result in impaired placental calcium transport and severe undermineralization and dysplasia of the fetal skeleton. American Journal of Medical Genetics Part A. 176(9). 1950–1955. 33 indexed citations

Bowden, Ramsay, Michael Parker, Jo Ellen Patterson, et al.. (2018). Extending the phenotype associated with the CSNK2A1‐related Okur–Chung syndrome—A clinical study of 11 individuals. American Journal of Medical Genetics Part A. 176(5). 1108–1114. 29 indexed citations

Kogelenberg, Margriet van, Alice R. Clark, Zandra A. Jenkins, et al.. (2015). Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA. Journal of Molecular Medicine. 93(7). 773–782. 9 indexed citations

Rankin, Julia, John Short, Peter D. Turnpenny, Bruce Castle, & C. Oliver Hanemann. (2013). Medulloblastoma in a patient with the PTPN11 p.Thr468Met mutation. American Journal of Medical Genetics Part A. 161(8). 2027–2029. 15 indexed citations

Richards, Allan J., Annie McNinch, David E. Hill, et al.. (2013). Alternative splicing modifies the effect of mutations in COL11A1 and results in recessive type 2 Stickler syndrome with profound hearing loss. Journal of Medical Genetics. 50(11). 765–771. 37 indexed citations

Szymańska, Katarzyna, Ian Berry, Clare V. Logan, et al.. (2012). Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies. SHILAP Revista de lepidopterología. 1(1). 18–18. 37 indexed citations

Turner, Claire, Deborah Mackay, Jonathan L A Callaway, et al.. (2010). Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci. European Journal of Human Genetics. 18(6). 648–655. 73 indexed citations

Plomp, Astrid S., Ralph J. Florijn, Bruce Castle, et al.. (2008). ABCC6 mutations in pseudoxanthoma elasticum: an update including eight novel ones.. PubMed. 14. 118–24. 28 indexed citations

10.

Barber, John, et al.. (2007). Transmitted duplication of 12q21.32–12q22 includes 48 genes and has no apparent phenotypic consequences. American Journal of Medical Genetics Part A. 143A(6). 615–618. 3 indexed citations

11.

Thomas, N. Simon, et al.. (2004). SHOX mutations in a family and a fetus with Langer mesomelic dwarfism. American Journal of Medical Genetics Part A. 128A(2). 179–184. 14 indexed citations

12.

MacKenzie, I.Z., et al.. (1989). Transfer of prostaglandins to the fetus after prostaglandin E2 vaginal pessary administration. American Journal of Obstetrics and Gynecology. 161(4). 920–923. 6 indexed citations

13.

MacKenzie, I.Z., Bruce Castle, M. Selinger, Jane F. Ferguson, & P. J. BOWELL. (1988). Serial fetal blood sampling for the management of pregnancies complicated by severe rhesus (D) isoimmunization. BJOG An International Journal of Obstetrics & Gynaecology. 95(8). 753–758. 29 indexed citations

14.

MacKenzie, I.Z., et al.. (1987). In‐utero intravascular transfusion of the fetus for the management of severe Rhesus isoimmunization—a reappraisal. BJOG An International Journal of Obstetrics & Gynaecology. 94(11). 1068–1073. 19 indexed citations

15.

MacKenzie, I.Z., et al.. (1987). Prostaglandin release from preparations used vaginally for the induction of labour. Prostaglandins. 34(6). 939–946. 17 indexed citations

16.

Brennecke, Shaun P., Bruce Castle, Laurence M. Demers, & A. C. Turnbull. (1985). Maternal plasma prostaglandin E₂ metabolite levels during human pregnancy and parturition. BJOG An International Journal of Obstetrics & Gynaecology. 92(4). 345–349. 25 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact